Dr.Reddys Laboratories Ltd Walk-in Interview.Dr.Reddys Laboratories Ltd Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue.
Important Details :
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
- Job Location: Hyderabad,baddi
Vacancy details:
- Department: Team Member – SIT (Quality Control)/Team Member – SIT (QC Microbiology)/Team Member – SIT (Engineering)
- Qualification: B.Pharm, M.Sc, M.Pharm/M.Sc. Microbiology
- Exp : 8-10 Years
Job Description : Greeting from Dr.Reddys Laboratories Ltd..!!!!
Team Member – SIT (Quality Control)
To involve from start and investigate level 2 & 3 incidents, by working closely with site CFT and operating people to arrive at proper Root cause, CA and PA and in report writing.
To Involve in valid OOS and other cases as relevant, by working closely with site CFT and operating people to arrive at proper Root cause, CA and PA and in report writing.
To review level 1B incidents and give feedback for improvement.
To periodically trend level 1A incidents and highlight/escalate key observations.
To review any other referred reports associated with incidents/events in association with sites.
To possess high level of integrity to have unbiased, independent and objective closure of incidents and maintain high level of confidentiality and have the tenacity to get to the root cause.
To use Rubrics template for investigation report writing.
To provide appropriate support to site in preparing for or during regulatory inspection for investigations.
looking someone with strong QC investigation background, QC Compliance, Analytical development
Education :B.Pharm, M.Sc, M.Pharm
Exp : 8-10 Years
Industry : OSD preferred/ Injectable, API also work
Team Member – SIT (QC Microbiology)
Job Summary
We are looking for an individual for the SIT Team to oversee the investigation of major and critical deviations, working closely with Cross-Functional Team (CFT) members to identify root causes and implement corrective and preventive actions. The role involves active participation in investigating Out of Specification (OOS) cases, ensuring accurate classification in the DCMS deviations log, and providing support during regulatory inspections.
Roles & Responsibilities
• You will be responsible for overseeing the investigation of major and critical deviations from the outset, collaborating closely with Cross-Functional Team (CFT) members to identify root causes, corrective actions (CA), preventive actions (PA), and preparing comprehensive reports. Your will also be working on the trending of the deviations and identification of adequate action items for reduction of the same.
• Your role involves active participation in investigating OOS (Out of Specification) and other relevant cases, working closely with CFT members to determine root causes, CA, PA, and report writing.
• You will review minor and critical , providing constructive feedback for improvement.
• Your responsibilities include periodically assessing the trending of minor deviations, highlighting or escalating key observations, regularly reviewing the deviations log to ensure accurate classification, and utilizing the Rubrics template for crafting investigation reports.
• You will offer necessary support to the site in readiness for or during regulatory inspections related to investigations.
Educational qualification: A Bachelor’s or Master’s degree in a relevant scientific field, such as Chemistry, Biochemistry, Pharmacy, or related discipline
Minimum work experience: 7 to 10 years of experience in a pharmaceutical or related industry with a focus on investigations and quality assurance
Skills & attributes:
Technical Skills
• In-depth knowledge and experience in overseeing investigations, and familiarity with root cause analysis, corrective actions (CA), and preventive actions (PA).
• Expertise in investigating valid OOS and other relevant cases.
• Familiarity with reviewing deviations / OOS log and ability to perform classification of data.
• Ability to craft comprehensive investigation reports.
• Experience in providing necessary support for regulatory inspections related to investigations.
• Knowledge of regulatory requirements pertaining to deviations investigations.
Behavioural Skills
• Ability to collaborate closely with CFT members.
• Analytical mind set for identifying root causes and developing effective solutions.
• Strong problem-solving skills and attention to detail in reviewing deviations, reports, and trending data and implementing corrective actions.
• Effective communication skills for report writing and escalation of key observations.
• Commitment to ensuring compliance with regulatory requirements in investigations.
• Ability to offer necessary support to the site in readiness for or during regulatory inspections.
looking someone with strong QC Microbiological investigation background.
Should have exp in Microbiological compliance.
Education :M.Sc. Microbiology
Exp : 8-10 Years
Industry : Injectable preferred/ OSD will be second preference
Person will be responsible to manage 3 sites Microbiological compliance at Badd
Team Member – SIT (Engineering)
Responsible for engineering related investigations. Engineering compliance or engineering investigation deviations,
Engineering SME for Audits
Education : B.Tech
From HVAC, Utility, qualification, water system, maintenance department
Exp : 8-10 Years
Industry : OSD preferred/ Injectable, API also work
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